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Article

Resource Utilization by Native and Invasive Earthworms and Their Effects on Soil Carbon and Nitrogen Dynamics in Puerto Rican Soils

1
Odum School of Ecology, University of Georgia, Athens, GA 30602, USA
2
Department of Biology, University of North Georgia, Dahlonega, GA 30597, USA
3
USDA Forest Service, International Institute of Tropical Forestry, Jardín Botánico Sur, 1201 Ceiba St., Río Piedras 00926, Puerto Rico
*
Author to whom correspondence should be addressed.
Forests 2016, 7(11), 277; https://doi.org/10.3390/f7110277
Submission received: 22 September 2016 / Revised: 5 November 2016 / Accepted: 6 November 2016 / Published: 15 November 2016
(This article belongs to the Special Issue Nutrient Cycling and Plant Nutrition in Forest Ecosystems)

Abstract

:
Resource utilization by earthworms affects soil C and N dynamics and further colonization of invasive earthworms. By applying 13C-labeled Tabebuia heterophylla leaves and 15N-labeled Andropogon glomeratus grass, we investigated resource utilization by three earthworm species (invasive endogeic Pontoscolex corethrurus, native anecic Estherella sp., and native endogeic Onychochaeta borincana) and their effects on soil C and N dynamics in Puerto Rican soils in a 22-day laboratory experiment. Changes of 13C/C and 15N/N in soils, earthworms, and microbial populations were analyzed to evaluate resource utilization by earthworms and their influences on C and N dynamics. Estherella spp. utilized the 13C-labeled litter; however, its utilization on the 13C-labeled litter reduced when cultivated with P. corethrurus and O. borincana. Both P. corethrurus and O. borincana utilized the 13C-labeled litter and 15C-labeled grass roots and root exudates. Pontoscolex corethrurus facilitated soil respiration by stimulating 13C-labeled microbial activity; however, this effect was suppressed possibly due to the changes in the microbial activities or community when coexisting with O. borincana. Increased soil N mineralization by individual Estherella spp. and O. borincana was reduced in the mixed-species treatments. The rapid population growth of P. corethrurus may increase competition pressure on food resources on the local earthworm community. The relevance of resource availability to the population growth of P. corethrurus and its significance as an invasive species is a topic in need of future research.

1. Introduction

Invasive earthworms have caused significant effects on local biota and ecosystem processes (such as nutrient dynamics) in the invaded areas, e.g., European Lumbricids in North America [1,2,3]. Population declines of native earthworms, particularly in remote and non-fragmented forests, have contributed to a result of competitive exclusion by expanding invasive earthworm populations [2,4,5]. Lachnicht et al. [6] observed that invasive Pontoscolex corethrurus (Müller, 1856) earthworms, when incubated with native Estherella sp., utilized different N resources, possibly avoiding direct competition on food resource. Winsome et al. [7] found that invasive Aporrectodea trapezoides (Dugès, 1828) lost its competition advantage when co-existing with native Argilophilus marmoratus (Eisen, 1893) in the resource-poor habitat of a Californian grassland. Interactions between native and invasive earthworms varied with resource utilization of earthworm species and resource availability [6,7]. Earthworms are categorized into three ecological groups, epigeic, endogeic, and anecic, based on their preferences on space and food resources [8]. Epigeic earthworms mainly consume leaf litter (and microbial populations colonizing on it) and inhabit the litter layer, while endogeic earthworms occupy mineral soils and use soil organic matter as their main food resources. Anecic earthworms utilize mainly leaf litter but with the ability to build burrows deep in the soil [8]. Earthworms with same feeding strategies are expected to evolve stronger competitive interactions because they share the same food resources [2,9,10]. Hence, resource utilization of earthworms could serve as a determinant for the success of earthworm invasions and its effects on the native earthworm community [7].
Earthworm invasions have significantly altered nutrient dynamics (e.g., carbon (C) and nitrogen (N)) in invaded soils [1,11,12]. A mixed-species of European Lumbricid earthworm assemblage has been documented to lessen organic layers and relocate leaf litter and humus fragments (C) into the deeper mineral soils, as well as to cause an increase of N loss in the soil adjacent to plant roots in the temperate forests of North America [1]. The effects of earthworms on soil C and N dynamics may vary with the feeding strategies of earthworms and composition of earthworm assemblages [13]. For example, epigeic earthworms may have stronger effects on nutrient fluxes between leaf litter layers and microbial populations that colonized on it (detritusphere) from their comminution and digestion of the leaf litter substrate [1,11,12]. Endogeic/anecic earthworms, on the other hand, may play a significant role in regulating nutrient dynamics in mineral soil and plant root zones (rhizosphere) by their consumption of soil organic matter and root exudates (and depositions) and their active burrowing activity [14,15,16]. In an area inhabited by a mixture of earthworms (either different feeding strategies or native co-existing with invasive worms), whether earthworm effects on soil nutrient dynamics can be explained by a summation of individual earthworm effects or disproportionally dominated by one aggressive earthworm species is a topic of interest, yet still in need of more research.
Stable isotope 13C and 15N techniques, including 13C- and 15N-labeled plant materials and a natural abundance of 13C and 15N isotopes, have recently provided invaluable information for studying earthworm feeding strategies and their effects on soil C and N dynamics [6,17,18,19,20]. For example, Hendrix et al. [17] suggested an inter-specific competition for N resources based on their observation of overlapped natural abundance 15N in both Estherella sp. and P. corethrurus in a lower altitude tabonuco forest, Puerto Rico. Neilson et al. [18] found that a natural abundance of 13C and 15N in earthworms can be used to assess the availability and diversity of food resources in the environment. With the application of 13C- and 15N-enriched plant materials, how earthworms utilize different type of food resources and the corresponding effects on soil C and N dynamics can be evaluated by tracking changes of δ13C and δ15N associated with 13C and 15N-labeled plant materials in soils, earthworms, and the microbial populations. In this study, we applied 13C-labeled Tabebuia heterophylla (DC.) Britton leaves and 15N-labeled Andropogon glomeratus (Walter) Britton, Sterns, & Poggenb. grass to investigate resource utilization of three earthworm species from Puerto Rico (invasive Pontoscolex corethrurus, native Estherella spp., and native Onychochaeta borincana (Borges, 1994) and their effects on soil C and N dynamics in Puerto Rican soils.
Pontoscolex corethrurus has invaded multiple habitats in Puerto Rico, in contrast to the restricted distribution of the native earthworms in mature forests [21,22]. Competition pressure from invasive P. corethrurus to native earthworms has been suggested to be responsible for the absence of native earthworms in most disturbed areas, i.e., pasture and young forests [22,23,24]. Lachnicht et al. [6] observed that endogeic P. corethrurus and anecic Estherella sp. showed resource partitioning (in terms of space and food) to avoiding direct competition in a 19-day laboratory experiment. The interactions observed between P. corethrurus and Estherella sp. have also caused differential influences on soil C and N mineralization [6]. In this study, we investigated feeding strategies of endogeic P. corethrurus, anecic Estherella sp., and endogeic Onychochaeta borincana (single-species earthworm treatments) on 13C-labeled Tabebuia leaves and 15N-labeled Andropogon grass. Changes in resource utilization of individual earthworm species would be evaluated by comparing earthworm tissue 13C and 15N of single-species earthworm treatments to those of mixed-species earthworm treatments (co-existed with other anecic/endogeic earthworms). Influences of individual earthworm species and inter-specific earthworm interactions on soil C and N dynamics would be assessed by tracking the changes of 13C and 15N in soils, earthworms, and microbial populations in single- and mixed-species earthworm treatments. Anecic Estherella spp. was expected to utilize more 13C-labeled Tabebuia leaves, as compared with endogeic O. borincana and endogeic P. corethrurus. Given that P. corethrurus is believed to exhibit flexible feeding behaviors and enhance soil mineralization [6,17], we expected that P. corethrurus would utilize more leaf litter (detritusphere) than plant roots (rhizosphere) resources, when incubated with endogeic O. borincana, to avoid competition with O. borincana. Higher population growth would be observed in a P. corethrurus population, which would enhance soil C and N mineralization. However, the presence of anecic Estherella sp. and endogeic O. borincana would weaken enhanced soil mineralization caused by P. corethrurus.

2. Materials and Methods

2.1. Experiment Design and Setup

The experiment was conducted at Sabana Field Research Station in Luquillo, Puerto Rico, from November to December 2006. A total of 60 soil mesocosms (Polyvinyl Chloride (PVC) material, 11 cm in diameter and 20 cm in depth) were set up with 15-cm-deep field soils with the bottoms sealed with a 1 mm mesh fiberglass window screen. Experimental treatments included (1) control mesocosms (n = 4, no earthworms; Control) with isotope-labeled Tabebuia litter and Andropogon glomeratus grass; and (2) seven earthworm treatments (each treatment: n = 4) with isotope-labeled Tabebuia litter and A. glomeratus grass: single and mixed earthworm treatments (two- and three-species earthworm combination; see below). Four soil mesocosms with no isotope-labeled plant materials and no earthworms (Soil; n = 4), four soil mesocosms with 15N-labeled grass plants (Grass; n = 4), and four soil mesocosms with 13C-labeled leaf litter (Litter; n = 4) were also analyzed as reference data to evaluate the efficiency of 13C- and 15N-labeled methods.
Experimental soil was collected from the forest at the Bisley Experimental Watersheds (BEW) in the Luquillo Mountains (18°18′ N; 65°50′ W). The forest at BEW is mostly dominated by a secondary growth of tabonuco trees, and its soils are clayey and well weathered Ultisols. Detailed description of BEW can be found in Scatena [25]. The collected soils were separated by three depths of 0–5, 5–10, and 10–15 cm to air-dry for 48 h and sieved through a 5 mm mesh size sieve to exclude plant roots, rocks, cocoons, and earthworms. Three depths of air-dry soils were used to set up the 0–5, 5–10, and 10–15 cm depth in the mesocosms. Total soil C and N in 0–5 cm were 3.96 ± 0.05% and 0.37%, respectively. Three Andropogon glomeratus seedlings (ca. 8 cm tall), the common grass species in Puerto Rico, were transplanted into each control and earthworm mesocosm a week before the beginning of the experiment. The Andropogon grass leaves were brushed with 2 atom % 15N-urea solution every day to establish 15N-labeled plant roots and root-derived substrates (the rhizosphere) during the experiment [26]. Seedlings of Tabebuia heterophylla, one of the common, native woody species (Family: Bignoniaceae) in Puerto Rico, were incubated in a growth chamber with pulse injection of 99 atom % 13CO2 to acquire 13C-labeled Tabebuia leaves through photosynthesis cycles during June–July 2006. After labeling procedures, Tabebuia senescent leaves were collected, air-dried for 48 hours, and then shredded into 1 cm2 pieces (δ13C varied from 385‰ to 804‰). A total of 3.7 g of dry 13C-labeled Tabebuia litter (calculated based on field litterfall data) was applied to the soil surface of each control and earthworm mesocosm to establish 13C-labeled litter and related microbial populations (detritusphere).

2.2. Earthworm Species and Collection

Three earthworm species from Puerto Rico were chosen for this experiment. Two native species, Estherella spp. and Onychochaeta borincana, were collected from the BEW forests (18.5°18′51.893″ N, 65.5°44′41.694″ W) and a riparian forest in Almirante Norte (18°41′ N, 65°38′ W; alluvial soil) in Puerto Rico [27], respectively; while Pontoscolex corethrurus was collected from the pasture at the Sabana Field Research Station (18°18′ N, 65°50′ W) in the town of Luquillo, Puerto Rico. Anecic Estherella spp. has dark pigmentation on the dorsal side and stays in leaf litter and upper soil layers. Endogeic O. borincana has pale coloration and stays in the subsoil layer. The invasive earthworm species, P. corethrurus, as an endogeic species, is the dominant peregrine earthworm that has colonized most habitats of Puerto Rico [6,17]. Before introducing into the earthworm mesocosms, gut contents of all earthworms were voided for 24 h, and their fresh biomass was recorded as the initial biomass data at the beginning of the experiment. Earthworms were introduced to assigned single or mixed earthworm treatments as followed: single species treatments—O. borincana only (O; 4 worms), Estherella spp. only (E; 4 worms), and P. corethrurus only (P; 4–5 worms); two-species mixed treatments—Estherella and P. corethrurus (E + P; 3 worms from each species), Estherella and O. borincana (E + O; 4 Estherella worms and 3 O. borincana worms), and O. borincana and P. corethrurus (O + P; 3 worms from each species); and three-species mixed treatments—Estherella, P. corethrurus, and O. borincana (E + P + O; 2 Estherella, 2 O. borincana, and 3 P. corethrurus). Four soil mesocosms were assigned to the control and each earthworm treatment as experimental replicates. The earthworm species were introduced into the experimental mesocosms following the order of O. borincana, Estherella spp., and P. corethrurus. Average fresh biomass of earthworms for each earthworm treatment is listed in Table 1. Each mesocosm was watered with 35 mL of water every day to maintain soil moisture during the 22-day experiment. The mesocosms were rotated randomly every week during the experiment.

2.3. Experiment Responding Variables

2.3.1. Soil CO2 and 13C-CO2

At Day 21 of the experiment, soil carbon dioxide (CO2) evolution was collected using the alkali absorption technique [28]. At each sampling, a circular area (5 cm in diameter) in between the center and the edge of the mesocosm was randomly chosen for each mesocosm, and the Tabebuia litter within was gently removed to the side. A PVC chamber (10 cm tall and 5 cm in diameter) was inserted 1 cm into the soil surface of each mesocosm with a scintillation vial containing 10 mL of a 1 mol/L NaOH solution placed inside each PVC chamber. The chamber was sealed with plastic wrap and aluminum foil on the top for soil CO2 absorption. Five NaOH solution vials (control) were kept closed during the 24 h absorption, except to open only at the beginning and the end of absorption to assess sampling contamination. Twenty-four hours later, each alkali solution was removed from the chamber, and 2 mL of 1 mol/L BaCl2 was added to form BaCO3 precipitate. Total CO2 trapped by alkali solution was determined by titration with 1 mol/L HCl to reach a pH neutral point (phenolphthalein endpoint) [28]. BaCO3 precipitate from each sample was air dried and packed in tin capsules for 13C-CO2 analysis.

2.3.2. The Remaining Mass of the Tabebuia Litter

Soil mesocosms were deconstructed at Day 22 to collect final data of the experiment. Tabebuia litter was carefully picked up and oven-dried at 60 °C for 48 h. The litter samples were ground, and a subsample of 0.5 g litter was burned at 550 °C for 4 h to obtain ash-free dry matter (AFDM) data. The data were used to calculate the remaining litter mass at the end of the experiment.

2.3.3. Survivorship, Growth, and the 13C and 15N Composition of Earthworms

The number of earthworms that survived at the end of the experiment was used to determine earthworm survivorship. All earthworms were put into separate containers to void their gut contents for 24 h. Final fresh biomass was recorded after gut-voiding. Earthworms were killed by dipping in boiling water for 3 seconds. One-third of the earthworm body (tail part) was cut and rinsed with deionized water with the gut content removed. Earthworm tissue was then freeze-dried and ground. Two milligrams of earthworm tissue was packed into a tin capsule and analyzed by dry combustion on a Carlo Erba NA1500 CN analyzer (Thermo Scientific, Waltham, MA, USA) for earthworm total C, N, and 13C and 15N.

2.3.4. Soil and Soil Microbes

Soil was separated into three soil depths, 0–5, 5–10, and 10–15 cm. Ten grams of soil from each depth was oven-dried at 105 °C for 48 h to calculate soil moisture. Subsamples of soils were ground and packed into tin capsules (ca. 20 mg) for total soil carbon (C) and nitrogen (N) and isotopic analysis (13C and 15N) by dry combustion on a Carlo Erba NA1500 CN analyzer. Two sets of 20 g 0–5 cm soils were extracted with 60 mL of a 0.5 mol/L potassium sulfate (K2SO4) solution (3:1 solution to soil mass ratio) for soil microbial biomass analysis by using the fumigation–extraction method [29,30]. Total microbial biomass C and 13C was analyzed from K2SO4-extracted samples using an OI analytical TIC/TOC analyzer (Shimaduz, Kyoto, Japan) coupled with a Thermo-Finnigan Delta Plus Isotope Ratio Mass Spectrometer (IRMS) (Thermo Scientific, Waltham, MA, USA). The persulfate digestion method was adapted to obtain microbial N data [31]. The K2SO4-extracted samples and persulfate digestion samples were analyzed with an Alpkem nitrogen autoanalyzer (OI analytical, College Station, TX, USA). Dissolved inorganic N (DIN; NH4+-N and NO3-N) was calculated from a non-fumigated K2SO4 extract. Microbial biomass N (MBN) was calculated from the difference between total persulfate nitrogen from fumigated and non-fumigated samples. Total persulfate nitrogen from fumigated samples was used to determine total dissolved nitrogen (TDN).
Delta 15N data for each portion (DIN, MBN, and TDN) were obtained by running the samples through the isotope diffusion method [32]. The δ13C/ δ15N value is calculated based on the measure isotope ratios between the samples and the standard:
δ 13C (‰) = ((RsampleRstandard) / Rstandard) × 103
δ 15N (‰) = ((RsampleRstandard) / Rstandard) × 103
where δ13C (δ15N) unit is the parts per thousand and R is the mass ratio of 13C/12C (15N/14N) in the sample and standard [33].
For DIN (K2SO4) extracts, KCl was added along with MgO and Devarda’s alloy to increase the ionic strength of the solution. For microbial N and TDN (persulfate digests) samples, 10 M NaOH was added to raise pH (>13) of the solution instead. Pairs of glass filter disks (Whatman GF/D) were prepared by baking in a muffle furnace at 500 °C for 4 h. They were acidified with 35 µL of 2M H2SO4 and then wrapped with Teflon tape. The Teflon-filter packages were incubated in the solutions for 6 days. After the incubation, the packages were dried over concentrated H2SO4 for at least 48 h, then packed in silver capsules for dry combustion on a Carlo Erba NA1500 CN analyzer and IRMS for total N and 15N data.

2.4. Statistic Analysis

The differences of litter remaining mass (data transformed), soil respiration (C-CO2, 13C-CO2, and δ13C), total C/N concentration, atom percentage of 13C/15N, and δ13C/ δ15N in soil, microbial biomass, and earthworm tissue, dissolved inorganic nitrogen (DIN), DIN-15N, and total dissolved nitrogen (TDN) between control and earthworm treatments were analyzed by a one-way ANOVA procedure (a generalized linear model (GLM) was used if data were not balanced) in SAS statistical software [34]. A GLM was also used to compare the differences of earthworm biomass and survivorship (data transformed) between earthworm treatments. If significantly different, Tukey’s HSD method was applied for the comparisons between treatments. Student’s t-test and GLM were applied to compare worm 13C and 15N differences between earthworm species in two-species and three-species mixed earthworm treatments, respectively. The significance level was set as α = 0.05.

3. Results

3.1. Litter Mass Loss and Soil C and N

The remaining mass of the Tabebuia litter (ash-free dry weight), ranging from 21.6% in the control treatment to 45.3% in the E + O earthworm mesocosms, was not significantly different between control and earthworm treatments (data transformed; GLM, F7, 31 = 2.1, p = 0.08). At the end of the experiment, soil total C and total N concentrations were not significantly different between the initial soil, the soil samples (with no worms), and earthworm treatments (soil C: F8, 27 = 1.0, p = 0.43; soil N: F8, 27 = 0.2, p = 0.9; Table 2). Soil carbon in the O + P earthworm mesocosms showed a significantly higher soil 13C percentage (1.0786 ± 0.002%) and soil 15N percentage (0.36915 ± 0.00072%), as compared with those in the initial soil (soil 13C = 1.0753 ± 0.0001% and soil 15N = 0.36815 ± 0.00005%) and the control soil (soil 13C = 1.0752 ± 0.0002% and soil 15N = 0.36810 ± 0.00005%) (both p < 0.01; Table 2). Soil C and N from the earthworm treatments showed stronger δ13C (average = −25.9 ± 0.9‰) and δ15N (average = 6.5 ± 1.0‰) signatures as compared with the control soil (δ13C= −27.9 ± 0.2‰ and δ15N = 4.5 ± 0.1‰).

3.2. Earthworm Populations

3.2.1. Earthworm Biomass and Survivorship

Average fresh biomass of the surviving earthworms for each earthworm treatment at the end of the 22-day mesocosm experiment is listed in Table 1. The endogeic earthworm, Onychochaeta borincana, showed significantly lower survivorship (71.8 ± 25.0%) than the other two earthworm species (epi-endogeic Pontoscolex corethrurus: 96.9 ± 8.3%; anecic Estherella spp.: 93.8 ± 13.0%) (data-transformed, GLM, F2, 47 = 9.56, p = 0.0003). However, the survivorship of individual earthworm species did not significantly differ between the single or the mixed-earthworm treatments (GLM, Estherella: F3, 15 = 1.6, p = 0.2; O. borincana: F3, 15 = 0.4, p = 0.8; P. corethrurus: F3, 15 = 0.7, p = 0.6), nor did the biomass changes (%) of individual earthworm species (Estherella: F3, 15 = 0.6, p = 0.7; O. borincana: F3, 15 = 1.1, p = 0.4; P. corethrurus: F3, 15 = 2.1, p = 0.2). A total of eight P. corethrurus were reproduced during the 22-day mesocosm experiment.

3.2.2. Tissue C/13C and N/15N in Native Estherella spp.

Percentage of tissue biomass C of anecic Estherella spp. showed no significant difference between its single species treatment (cultivated alone; tissue C = 46.3 ± 0.3%) and the mixed-species treatments (cultivated with O. borincana and/or P. corethrurus; tissue C (%) = 45.7%–47.2%) (F3, 39 = 2.2, p = 0.1; Table 3). However, Estherella spp. when cultivated alone was found to have significantly higher 13C enrichment (as in δ13C and atom percentage of 13C) as compared with the mixed-species treatments (for δ13C: E + P and E + O + P mesocosms; F3, 39 = 2.0, p = 0.04) (for tissue 13C (%): E + P mesocosms; F3, 39 = 2.9, p = 0.047) (Table 3). Estherella spp. did not show a significant difference in worm tissue N (%), δ15N, and 15N (%) between its single species and the mixed-species mesocosms (all p > 0.4; Table 3).

3.2.3. Tissue C/13C and N/15N in Native O. Borincana.

For endogeic O. borincana, there was no significant difference in worm tissue C and N (%), δ13C and δ15N signatures, and tissue 13C and 15N (%) between its own single species and the mixed-species mesocosms (all p > 0.2; see Table 3).

3.2.4. Tissue C/13C and N/15N in Invasive P. corethrurus

Invasive P. corethrurus earthworms did not show significant differences in worm tissue C and N (%), δ13C and δ15N enrichments, and tissue 13C and 15N (%) between its single species and the mixed-species mesocosms (all p > 0.2; Table 4). However, the juvenile P. corethrurus reproduced during this 22-day mesocosm experiment did show significant lower tissue C (41.0 ± 4.7%) and N percentages (9.2 ± 2.0%), as compared with the adult P. corethrurus worms (tissue C (%): F4, 52 = 3.9, p = 0.007; tissue N (%): F4, 52 = 6.0, p < 0.001) (Table 4). Juvenile P. corethrurus worms also showed lower enrichment of δ13C (−24.3 ± 1.4‰) and tissue 13C (1.0791 ± 0.0011%), as compared with the adult P. corethrurus worms (δ13C: F4, 52 = 4.7, p =0.002; tissue 13C (%): F4, 52 = 4.8, p =0.002) (Table 4). There was a significantly higher enrichment of 15N (as in δ15N = 7.6 ± 0.9‰ and an atom percentage of 15N = 0.3692 ± 0.0003%), as compared with the adult P. corethrurus worms (δ15N: F4, 52 = 7.2, p < 0.001; atom percentage 15N: F4, 52 = 7.2, p < 0.001) (Table 4).

3.3. Microbial Biomass Carbon and Soil Respiration

There was no significant difference in microbial biomass carbon (MBC) and MBC-13C between the soil (MBC = 741.3 ± 103.0 ug C g−1 soil; MBC-13C = 8.0 ± 1.1 ug C g−1 soil), control (MBC = 332.1 ± 183.2 ug C g−1 soil; MBC-13C = 3.6 ± 1.3 ug C g−1 soil), and earthworm treatments (MBC ranged from 340.1 to 532.1 ug C g−1 soil; MBC-13C from 3.7 to 7.2 ug C g−1 soil) (MBC: F10, 29 = 1.3, p = 0.26; MBC-13C: F10, 29 = 1.3, p = 0.27; Table 5). Microbial biomass 13C (%) was significantly higher in the control treatments, as compared with those in the Soil Only or Grass mesocosms (F10, 29 = 2.8, p = 0.015; Table 5), which suggested the microbes utilized and incorporated the 13C-labeled litter into their biomass. The microbial biomass δ13C enrichment from P (−28.8 ± 3.4‰), O + P (−28.8 ± 3.4‰), and E + O + P (−29.1 ± 2.5‰) treatments were significantly higher than the Soil Only treatment (−36.1 ± 1.4‰) (F10, 29 = 3.3, p = 0.006; Table 5).
At the end of the experiment (Day 21), soil respiration C-CO2 and 13C-CO2 (%) from the control (soil with both 13C- and 15N-labeled materials but no worms) and the earthworm treatments were significantly higher than the Soil Only and Grass treatments (both p < 0.0001; Table 5). This suggested that the input of 13C-labeled leaf-litter and earthworms facilitated microbial respiration. However, different earthworm treatments showed differential effects on 13C-CO2 (%) evolved in the microbial respiration. The P. corethrurus earthworm treatment showed higher 13C evolved from the microbial respiration (as in 13C-CO2 and δ13C; Table 5) as compared with that from the O + P earthworm treatment at the end of the experiment (both p < 0.0001; Table 5).

3.4. Soil and Microbial Nitrogen Dynamics

There was no significant difference in microbial biomass nitrogen (MBN) between the control and earthworm treatments. However, the higher MBN-15N and microbial δ15N signature from the Grass treatment, compared with those in the control and earthworm treatments (except E + O treatment), indicated that the microbes did utilize and incorporate the 15N-labeled grass resources (plant roots or root exudates) into the microbial biomass (both p < 0.0001; Table 6).
At the end of experiment (Day 21), lower soil dissolved inorganic nitrogen (DIN) was found in the control and the earthworm treatments, except native Estherella spp. (E) and O. borincana (O) treatments, as compared with the Soil Only mesocosms (F10, 31 = 5.7, p < 0.0001; Table 6). Earthworms not only reduced the DIN in the experimental soil but also reduced the 15N percentage in DIN (except O + P treatment) (F10, 31 = 6.4, p < 0.0001; Table 6). There was no significant difference total dissolved nitrogen (TDN) between the control (10.8 ± 1.5 μg N/g soil) and the earthworm treatments (ranged from 12.0–17.1 μg N/g soil) (F10, 31 = 1.3, p = 0.3).

4. Discussion

In this study, newly added 13C-labeled leaf litter and 15N-labeled grass were sufficiently incorporated into 10 cm of top soil, soil microbial biomass, and earthworm tissue. Natural abundance of δ13C in earthworms was suggested to be 1−3‰ heavier than its dietary sources (such as leaf litter, root exudates, and microbial populations in the soil) [18,35]. In this study, earthworm δ13C showed on average 1.4‰ heavier in Estherella spp., 3.5‰ heavier in P. corethrurus, and 5‰ heavier in O. borincana, with respect to the soil δ13C, while earthworm tissue showed on average 5.9‰ heavier δ13C in Estherella spp., 7.2‰ heavier in P. corethrurus, and 8.5‰ heavier in O. borincana than the microbial biomass δ13C in which they inhabited (Table 2, Table 3, Table 4 and Table 5).
We did not observe any competition exclusion among three earthworm species based on the survivorship and biomass gain among the single-species and the mixed-species treatments for each individual species. However, anecic Estherella spp., when cultivated alone, did show higher tissue—13C (%) and δ13C—compared with when it was cultivated with other earthworm species. This suggested that Estherella spp. might change its feeding strategy by reducing its utilization of 13C-labeled litter materials and/or the microbial community that was related to the 13C-labeled litter when cultivated with P. corethrurus or both P. corethrurus and O. borincana. Lachnicht et al. [6] observed that P. corethrurus and Estherella spp., while cultivated together, excluded each other in the bottom and upper layers of soil, respectively, in a 19-day laboratory experiment in Puerto Rican soils. The authors also found that P. corethrurus acquired more 15N-labeled leaf litter when co-occurring with Estherella spp. [6]. We did not find that P. corethrurus changed its feeding preference in this 22-day experiment based on worm tissue 13C and δ13C as well as tissue 15N and δ15N between the single-species and mixed-species earthworm treatments, nor did O. borincana. In this study, cultivating live A. glomeratus grass plants could provide a steady, continuous supply of root exudates and rhizodeposits for soil microbes and earthworms, as compared to the one-time application of 13C-labeled glucose and 15N-labeled leaf litter adopted by Lachnicht et al. [6]. Such a continuous supply of food resources might relieve potential inter-specific competitive pressure derived from limited food resources in short-term experiments, especially for endogeic earthworms like O. borincana and P. corethrurus that strongly rely on rhizosphere resources.
Both endogeic O. borincana and P. corethrurus showed 5‰ or higher δ13C signature than their food resources (soil organic matter and soil microbial biomass). Higher δ13C signature in both endogeic earthworms could be explained by their utilization on soil microbial populations (i.e., bacteria and fungi) as food resources. Fungal species (such as mycorrhizal and saprotrophic fungi) have been reported to have a higher 13C enrichment than plant foliage, fine roots, and soils because of fungal biochemical synthesis and transport between plant parts [36]. Microbial activity releases the lighter 12C in respiration and gradually results in an increase of 13C concentration in humified residues and its own population [37,38]. As a result, endogeic earthworms (active in rhizosphere and the mineral soils), P. corethrurus and O. borincana in this study, showed higher δ13C signature and tissue 13C (%) than anecic Estherella spp. due to their preferential consumption of 13C-enriched decayed/humified debris in the mineral soil layer, to a significant portion of 13C-enriched microbial (higher microbial δ13C observed in P, O + P and E + O + P earthworm treatments; Table 5) and fungal populations, or to both [6,36,37]. The possibility that both endogeic O. borincana and P. corethrurus consumed the microbial populations in the mineral soil, the rhizosphere, or both is also confirmed by their heavier δ15N signatures (0.6‰ and 2.7‰ δ15N heavier, respectively) compared with the soil δ15N (Table 2,Table 3 and Table 4).
We found that soil microbial-δ15N was on average 6.1‰ heavier than Estherella spp., 5.8‰ heavier than P. corethrurus, and 2.6‰ heavier than O. borincana (Table 3, Table 4 and Table 6). The stronger 15N enrichment in endogeic O. borincana could be derived from its utilization of 15N-labeled rhizosphere (plant roots, root exudates, and rhizosphere-related microbes). Even though no study has yet investigated the feeding behavior of O. borincana, some endogeic earthworms (e.g., P. corethrurus) are often found aggregated in the root zones utilizing living root fragments and dead root cells, or as response to enhanced microbial activities in the rhizosphere [35,39]. In this study, the presence of O. borincana seemed to relate to higher microbial biomass 15N and δ15N (in the E + O earthworm mesocosms) and higher DIN and higher 15N-DIN (%) in the O + P treatment (although not statistically significant), as compared with other earthworm treatments (Table 6). The potential effect of endogeic O. borincana on rhizospheric microbial populations and activities is a topic of interest, yet in need for further research.
Pontoscolex corethrurus showed a prolific reproduction (a total of eight juvenile P. corethrurus) within the 22-day soil mesocosm experiment. The stronger δ15N signal observed in juvenile P. corethrurus, as compared with the adults, might be explained by (1) the possibility that adult P. corethrurus allocated its assimilated 15N into cocoon reproduction, which later integrated into the tissue of juvenile P. corethrurus, and (2) a higher soil consumption and biomass increase in relation to overall biomass by juvenile worms than the adult worms [6]. Pontoscolex corethrurus has been described as one of the cosmopolitan earthworm species that has aggressively invaded many regions in the tropics, including Puerto Rico, Central Amazonian, and Peruvian soils [40,41,42,43]. Exceptional reproductive strategies of P. corethrurus, such as a high rate of cocoon production and hatching success, a short development time, and the ability of parthenogenesis, critically influence the local native earthworm community in the invaded soils [2]. The rapid population growth of P. corethrurus may increase competition pressure on food resources to the local native earthworm community [22]. The relevance of resource availability to the population growth of P. corethrurus and its significance in a P. corethrurus invasion is certainly a topic in need of future research.
Earthworms showed differential effects on soil mineralization processes in this study. All earthworm treatments along with the control (no worms) had higher soil respiration C-CO2 at Day 21, especially in the P, E + O, and O + P treatments, as compared with other control treatments (Soil Only, Grass, and Litter mesocosms). There were higher 13C-CO2 (%) and δ13C from the P mesocosms (Tukey’s HSD, p < 0.001) and the mixed E + O mesocosms (marginally significant; p = 0.06) compared with those from the O + P treatments. The effects on soil microbial activities by earthworms could be explained by earthworms’ direct grazing behavior on soil microbial community or indirect burrowing and casting activities [11,14]. Whether the higher soil respiration C-CO2 from the control (no worms) mesocosms was due to the release from earthworms’ grazing activity is uncertain. However, the significantly higher soil respiration 13C-CO2 (%) and δ13C from P. corethrurus (includes P and E + P) were an indicator of facilitating effects of earthworms on the enriched soil microbial biomass δ13C from the same mesocosms. Pontoscolex corethrurus might cause an increase in soil respiration via its simulation on the activity of the 13C-labeled microbial population. However, the lower soil respiration 13C-CO2 (%) and δ13C in the mixed P. corethrurus and O. borincana treatments (i.e., O + P) suggested that the presence of O. borincana and its interaction with P. corethrurus might have a negative effect on the 13C-labeled microbial community and facilitate the 15N-labeled microbial communities in the rhizosphere. Such a possibility is supported by the observation of the slightly increased 15N (%) in the soil DIN from the increased microbial activity related to the 15N-labeled rhizosphere in the O + P treatment (Table 6).
The individual stimulation on soil N mineralization by Estherella spp. and O. borincana was slightly reduced when they were incubated with other earthworm species (mixed-species earthworm treatments; Table 6). No significant change was observed in microbial biomass (C and N) between treatments, thus the changes shown in soil respiration δ13C and DIN could be explained by the changed activities from the microbial population or possibly alternation of microbial community induced by the inter-specific earthworm interactions from the mixed earthworm treatments. Studies have suggested that the preference of earthworms on utilizing different food resources can reshape microbial communities in the detritusphere and the rhizosphere [44,45]. Native Estherella spp. and O. borincana may individually sustain a microbial community that specialized on N mineralization in the rhizopshere, yet the microbes switched to those which utilized a labile, newly added 13C-labeled resource when sharing resources with the other species. Earthworm effect on either microbial activities or microbial community by individual species is confounded when inter-specific interactions are considered, and the individual effect on microbial activities and communities was not additive. Furthermore, changes in microbial activities and alterations to the microbial community by earthworms could gradually alter soil nutrient dynamics and availability of labile C and N over time [46], which later has an effect on habitat suitability for other species. For example, invasive Amynthas agrestis (Goto and Hatai, 1899) was documented to change soil microbial communities, which positively affected the habitat invasibility for another invasive species, Lumbricus rubellus (Hoffmeister, 1843) [47]. Many studies have focused on the earthworm effects on soil microbial biomass and soil mineralization [11,47,48,49,50,51,52,53]; however, research investigating the effects of earthworms with different feeding strategies (i.e., epigeic, anecic, and endogeic) on soil microbial activities and communities in terms of functional groups is still limited.

5. Conclusions

In this study, anecic Estherella spp. was observed to reduce its utilization on 13C-labeled litter or 13C-related microbial community when cultivated with P. corethrurus or both P. corethrurus and O. borincana. Resource utilization by different earthworms changed the activities and composition of soil microbial community and further affected soil respiration and nitrogen mineralization processes. However, the individual species effect on soil C and N dynamics was altered with mixed earthworm assemblages. Pontoscolex corethrurus was found to stimulate soil respiration by facilitating the activity of the 13C-labeled microbial activity; however, the positive effect was suppressed when it coexisted with O. borincana. The stimulated N mineralization process by native Estherella spp. and O. borincana individually were reduced when each of them cultivated with other earthworm species. We concluded that the earthworm effect on soil microbial community and activity varies by species, and the individual species effect is not additive when considering multiple earthworm species assemblages. Regulation on soil nutrient dynamics by native Estherella sp. and O. borincana may potentially affect habitat suitability (e.g., resource availability) to invasive P. corethrurus during colonization. However, the rapid population growth of P. corethrurus may increase competition pressure on food resources to the local earthworm community. The relevance of resource availability to the population growth of P. corethrurus and its significance as an invasive species is a topic in need of future research.

Acknowledgments

We thank the staff at the Sabana Field Research Station and the International Institute of Tropical Forestry (IITF) for their help in the lab and in the field. We also thank David Kissel, the Soil Plant and Water Laboratory and the University of Georgia, for helping us with the soil transportation and sterilization process. This research was supported by the National Science Foundation grant number 0236276 to the University of Georgia Research Foundation, Inc.; the Graduate Student Research Prize, Center for Biodiversity and Ecosystem Processes, University of Georgia; grant DEB-0218039 from the NSF to the Institute of Tropical Ecosystem Studies, University of Puerto Rico, and the USDA Forest Service-IITF as part of the LTER program in the Luquillo Experimental Forest. All research at the USDA Forest Service International Institute of Tropical Forestry was performed in collaboration with the University of Puerto Rico. We also thank Ariel E. Lugo, Frank Wadsworth, and two anonymous reviewers, for their comments and suggestions on an earlier version of this manuscript.

Author Contributions

Ching-Yu Huang and Paul F. Hendrix conceived the study and designed the experiment. Grizelle González provided field site information and aided in field site selection and field sample collection. Ching-Yu Huang processed the samples, analyzed the data, and prepared the manuscript. Paul F. Hendrix and Grizelle González provided suggestions and reviews at various stages of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Frelich, L.E.; Hale, C.M.; Scheu, S.; Holdsworth, A.R.; Heneghan, L.; Bohlen, P.J.; Reich, P.B. Earthworm invasion into previously earthworm-free temperate and boreal forests. Biol. Invasions 2006, 8, 1235–1245. [Google Scholar] [CrossRef]
  2. Hendrix, P.F.; Baker, G.H.; Callaham, M.A., Jr.; Damoff, G.A.; Fragoso, C.; Gonzaléz, G.; Winsome, T.; Zou, X. Invasion of exotic earthworms into ecosystems inhabited by native earthworms. Biol. Invasions 2006, 8, 1287–1300. [Google Scholar] [CrossRef]
  3. Hendrix, P.F.; Callaham, M.A., Jr.; Drake, J.M.; Huang, C.-Y.; James, S.W.; Snyder, B.A.; Zhang, W. Pandora’s box contained bait: The global problem of introduced earthworms. Annu. Rev. Ecol. Evol. Syst. 2008, 39, 593–613. [Google Scholar] [CrossRef]
  4. Callaham, M.A., Jr.; Hendrix, P.F.; Phillips, R.J. Occurrence of an exotic earthworm (Amynthas agrestis) in undisturbed soils of the southern Appalachian mountains, USA. Pedobiologia 2003, 47, 466–470. [Google Scholar] [CrossRef]
  5. Kalisz, P.J.; Wood, H.B. Native and exotic earthworms in wildland ecosystems. In Earthworm Ecology and Biogeography in North America, 1st ed.; Hendrix, P.F., Ed.; Lewis Publishers: Boca Raton, FL, USA, 1995; pp. 117–126. [Google Scholar]
  6. Lachnicht, S.L.; Hendrix, P.F.; Zou, X. Interactive effects of native and exotic earthworms on resource use and nutrient mineralization in a tropical wet forest soil of Puerto Rico. Biol. Fertil. Soils 2002, 36, 43–52. [Google Scholar] [CrossRef]
  7. Winsome, T.; Epstein, L.; Hendrix, P.F.; Horwath, W.R. Competitive interactions between native and exotic earthworm species as influenced by habitat quality in a California grassland. Appl. Soil. Ecol. 2006, 32, 38–53. [Google Scholar] [CrossRef]
  8. Bouché, M.B. Strategies Lombriciennes. In Soil Organisms as Components of Ecosystems: Proceedings of the VI International Soil Zoology Colloquium of the International Society of Soil Science (ISSS); Lohm, U., Persson, T., Eds.; Swedish Natural Science Research Council: Stockholm, Sweden, 1977; pp. 122–132. [Google Scholar]
  9. Lavelle, P.; Barois, I.; Cruz, I.; Fragoso, C.; Hernandez, A.; Pineda, A.; Rangel, P. Adaptive strategies of Pontoscolex corethrurus (Glossoscolecidae, Oligochaeta), a peregrine geophagous earthworm of the humid tropics. Biol. Fertil. Soils 1987, 5, 188–194. [Google Scholar] [CrossRef]
  10. Lavelle, P.; Lapied, E. Endangered earthworms of Amazonia: An homage to Gilberto Righi. Pedobiologia 2003, 47, 419–417. [Google Scholar] [CrossRef]
  11. Groffman, P.M.; Bohlen, P.J.; Fisk, M.C.; Fahey, T.J. Exotic earthworm invasion and microbial biomass in temperate forest soils. Ecosystems 2004, 7, 43–54. [Google Scholar] [CrossRef]
  12. Hale, C.M.; Frelich, L.E.; Reich, P.B.; Pastor, J. Effects of European earthworm invasion on soil characteristics in Northern hardwood forests of Minnesota, USA. Ecosystems 2005, 8, 911–927. [Google Scholar] [CrossRef]
  13. Huang, C.-Y.; Hendrix, P.F.; Fahey, T.J.; Bohlen, P.J.; Groffman, P.M. A simulation model to evaluate the impacts of invasive earthworms on soil carbon dynamics. Ecol. Model 2010, 20, 2447–2457. [Google Scholar] [CrossRef]
  14. Bossuyt, H.; Six, J.; Hendrix, P.F. Rapid incorporation of carbon from fresh residues into newly formed stable microaggregates within earthworm casts. Eur. J. Soil Sci. 2004, 55, 393–399. [Google Scholar] [CrossRef]
  15. Curry, J.P.; Schmidt, O. The feeding ecology of earthworms—A review. Pedobiologia 2007, 50, 463–477. [Google Scholar] [CrossRef]
  16. Mummey, D.L.; Rillig, M.C.; Six, J. Endogeic earthworms differentially influence bacterial communities associated with different soil aggregate size fractions. Soil Biol. Biochem. 2006, 38, 1608–1614. [Google Scholar] [CrossRef]
  17. Hendrix, P.F.; Lachnicht, S.L.; Callaham, M.A., Jr.; Zou, X. Stable isotopic studies of earthworm feeding ecology in tropical ecosystems of Puerto Rico. Rapid Commun. Mass Sp. 1999, 13, 1295–1299. [Google Scholar] [CrossRef]
  18. Neilson, R.; Boag, B.; Simth, M. Earthworm δ13C and δ15C analyses suggest that putative functional classifications of earthworms are site-specific and may also indicate habitat diversity. Soil Biol. Biochem. 2000, 32, 1053–1061. [Google Scholar] [CrossRef]
  19. Schmidt, O.; Scrimgeour, C.M.; Handley, L.L. Natural abundance of 15N and 13C in earthworms from a wheat and a wheat-clover field. Soil Biol. Biochem. 1997, 29, 1301–1308. [Google Scholar] [CrossRef]
  20. Zhang, W.; Hendrix, P.F.; Snyder, B.A.; Molina, M.; Li, J.; Rao, X.; Siemann, E.; Fu, S. Dietary flexibility aids Asian earthworm invasion in North American forests. Ecology 2010, 91, 2070–2079. [Google Scholar] [CrossRef] [PubMed]
  21. Gonzaléz, G.; Zou, X.; Borges, S. Earthworm abundance and species composition in abandoned tropical croplands: Comparison of tree plantations and secondary forests. Pedobiologia 1996, 40, 385–391. [Google Scholar]
  22. Sánchez-de León, Y.; Zou, X.; Borges, S.; Ruan, H. Recovery of native earthworms in abandoned tropical pastures. Conserv. Biol. 2003, 17, 999–1006. [Google Scholar] [CrossRef]
  23. Gonzaléz, G.; Zou, X.; Sabat, A.; Fetcher, N. Earthworm abundance and distribution pattern in contrasting plant communities within a tropical wet forest in Puerto Rico. Caribb. J. Sci. 1999, 35, 93–100. [Google Scholar]
  24. Huang, C.-Y.; Gonzaléz, G.; Hendrix, P.F. The re-colonization ability of native earthworm, Estherella spp., in Puerto Rican forests and pastures. Caribb. J. Sci. 2006, 42, 386–396. [Google Scholar]
  25. Scatena, F.N. An Introduction to the Physiography and History of the Bisley Experimental Watersheds in the Luquillo Mountains of Puerto Rico. Available online: www.srs.fs.usda.gov/pubs/gtr/gtr_so072.pdf (accessed on 19 September 2016).
  26. Schmidt, O.; Scrimgeour, C.M. A simple urea leaf-feeding method for the production of 13C and 15N labelled plant material. Plant Soil 2001, 229, 197–202. [Google Scholar] [CrossRef]
  27. Abelleira, O.J. Ecology of Novel Forests Dominated by the African Tulip Tree (Spathodea campanulata Beauv.) in Northcentral Puerto Rico. Master’s Thesis, University of Puerto Rico, Rio Piedras, Puerto Rico, 2009. [Google Scholar]
  28. Liu, Z.G.; Zou, X.M. Exotic earthworms accelerate plant litter decomposition in a Puerto Rican pasture and a wet forest. Ecol. Appl. 2002, 12, 1406–1417. [Google Scholar] [CrossRef]
  29. Joergensen, R.G. The fumigation-extraction method to estimate soil microbial biomass: Calibration of the kEC value. Soil Biol. Biochem. 1996, 28, 25–31. [Google Scholar] [CrossRef]
  30. Sparling, G.P.; West, A.W. A direct extraction method to estimate soil microbial C: Calibration in situ using microbial respiration and 14C labelled cells. Soil Biol. Biochem. 1988, 20, 337–343. [Google Scholar] [CrossRef]
  31. Cabrera, M.L.; Beare, M.H. Alkaline persulfate oxidation for determining total nitrogen in microbial biomass extracts. Soil Sci. Soc. Am. J. 1993, 57, 1007–1012. [Google Scholar] [CrossRef]
  32. Stark, J.M.; Hart, S.C. Diffusion technique for preparing salt solutions, Kjeldahl digests, and persulfate digests for nitorgen-15 analysis. Soil Sci. Soc. Am. J. 1996, 60, 1846–1855. [Google Scholar] [CrossRef]
  33. Coleman, D.C.; Fry, B. Carbon isotope techniques, 1st ed.; Academic Press, Inc.: San Diego, CA, USA, 1991. [Google Scholar]
  34. SAS Institute Inc. SAS Technical Report, SAS/STAT Software: The GLM Procedure; Version 6; SAS Institute Inc.: Cary, NC, USA, 1991; p. 217. [Google Scholar]
  35. Spain, A.V.; Saffigna, P.G.; Wood, A.W. Tissue carbon sources for Pontoscolex corethrurus (Oligochaeta: Glossoscolecidae) in a sugarcane ecosystem. Soil Biol. Biochem. 1990, 22, 703–706. [Google Scholar] [CrossRef]
  36. Hobbie, E.A.; Macko, S.A.; Shugart, H.H. Insights into nitrogen and carbon dynamics of ectomycorrhizal and saprotrophic fungi from isotopic evidence. Oecologia 1999, 118, 353–360. [Google Scholar] [CrossRef]
  37. Pollierer, M.M.; Langel, R.; Scheu, S.; Maraun, M. Compartmentalization of the soil animal food web as indicated by dual analysis of stable isotope ratios (15N/14N and 13C/12C). Soil Biol. Biochem. 2009, 41, 1221–1226. [Google Scholar] [CrossRef]
  38. Dijkstra, P.; Ishizu, A.; Doucett, R.; Hart, S.C.; Schwartz, E.; Menyailo, O.V.; Hungate, B.A. 13C and 15N natural abundance of the soil microbial biomass. Soil Biol. Biochem. 2006, 38, 3257–3266. [Google Scholar] [CrossRef]
  39. Binet, F.; Hallaire, V.; Curmi, P. Agricultural practices and the spatial distribution of earthworms in maize fields. Relationships between earthworm abundance, maize plants and soil compaction. Soil Biol. Biochem. 1997, 29, 577–583. [Google Scholar] [CrossRef]
  40. Chauvel, A.; Grimaldi, M.; Barros, E.; Blanchart, E.; Desjardins, T.; Sarrazin, M.; Lavelle, P. Pasture damage by an Amazonian earthworm. Nature 1999, 398, 32–33. [Google Scholar] [CrossRef]
  41. Fragoso, C.; Kanyonyo, J.; Moreno, A.; Senapati, B.K.; Blanchart, E.; Rodríguez, C. A survey of tropical earthworms: Taxonomy, biogeography and environmental plasticity. In Earthworm management in tropical agroecosystems; Lavelle, P., Brussaard, L., Hendrix, P., Eds.; CABI: New York, NY, USA, 1999; pp. 1–26. [Google Scholar]
  42. Gonzaléz, G.; Huang, C.-Y.; Zou, X.; Rodriguez, C. Earthworm invasions in the tropics. Biol. Invasions 2006, 8, 1247–1256. [Google Scholar] [CrossRef]
  43. Hallaire, V.; Curmi, P.; Duboisset, A.; Lavelle, P.; Pashanasi, B. Soil structure changes induced by the tropical earthworm Pontoscolex corethrurus and organic inputs in a Peruvian ultisol. Euro. J. Soil Biol. 2000, 36, 35–44. [Google Scholar] [CrossRef]
  44. Butenschoen, O.; Marhan, S.; Scheu, S. Response of soil microorganisms and endogeic earthworms to cutting of grassland plants in a laboratory experiment. Appl. Soil Ecol. 2008, 38, 152–160. [Google Scholar] [CrossRef]
  45. Sheehan, C.; Kirwan, L.; Connolly, J.; Bolger, T. The effects of earthworm functional diversity of microbial biomass and the microbial community level physiological profile of soils. Euro. J. Soil Biol. 2008, 44, 65–70. [Google Scholar] [CrossRef]
  46. Bohlen, P.J.; Edwards, C.A.; Zhang, Q.; Parmelee, R.W.; Allen, M. Indirect effects of earthworms on microbial assimilation of labile carbon. App. Soil Ecol. 2002, 20, 255–261. [Google Scholar] [CrossRef]
  47. Zhang, B.-G.; Li, G.-T.; Shen, T.-S.; Wang, J.-K.; Sun, Z. Changes in microbial C, N, and P and enzyme activities in soil incubated with the earthworms Metaphire guillelmi or Eisenia fetida. Soil Biol. Biochem. 2000, 32, 2055–2062. [Google Scholar] [CrossRef]
  48. Bohlen, P.J.; Scheu, S.; Hale, C.M.; McLean, M.A.; Migge, S.; Groffman, P.M.; Parkinson, D. Non-native invasive earthworms as agents of change in northern temperate forests. Front. Ecol. Environ. 2004, 2, 427–435. [Google Scholar] [CrossRef]
  49. Eisenhauer, N.; Partsch, S.; Parkinson, D.; Scheu, S. Invasion of a deciduous forest by earthworms: Changes in soil chemistry, microflora, microarthopods and vegetation. Soil Biol. Biochem. 2007, 39, 1099–1110. [Google Scholar] [CrossRef]
  50. Fisk, M.C.; Fahey, T.J.; Groffman, P.M.; Bohlen, P.J. Earthworm invasion, fine-root distributions, and soil respiration in North temperate forests. Ecosystems 2004, 7, 55–62. [Google Scholar] [CrossRef]
  51. Lachnicht, S.L.; Hendrix, P.F. Interaction of the earthworm Diplocardia mississippiensis (Megascolecidae) with microbial and nutrient dynamics in a subtropical Spodosol. Soil Biol. Biochem. 2001, 33, 1411–1417. [Google Scholar] [CrossRef]
  52. Li, X.; Fisk, M.C.; Fahey, T.J.; Bohlen, P.J. Influence of earthworm invasion on soil microbial biomass and activity in a northern hardwood forest. Soil Biol. Biochem. 2002, 34, 1929–1937. [Google Scholar] [CrossRef]
  53. Wolters, V.; Joergensen, R.G. Microbial carbon turnover in beech forest soils worked by Aporrectodea caliginosa (Savigny) (Oligochaeta: Lumbricidae). Soil Biol. Biochem. 1992, 24, 171–177. [Google Scholar] [CrossRef]
Table 1. Average fresh biomass of Estherella spp. (E), Onychochaeta borincana (O), and Pontoscolex corethrurus (P) earthworms introduced into different earthworm mesocosm (g per mesocosm).
Table 1. Average fresh biomass of Estherella spp. (E), Onychochaeta borincana (O), and Pontoscolex corethrurus (P) earthworms introduced into different earthworm mesocosm (g per mesocosm).
Earthworm Treatments
VariablesSingle species (E, O, P)E + OE + PO + PE + O + P
Estherella spp.
Fresh weight (before)5.3 (0.5)4.2 (0.6)3.2 (0.4)n/a2.2 (0.2)
Fresh weight (after)4.6 (1.2)3.9 (1.1)2.7 (0.6)n/a2.3 (0.4)
Onychochaeta borincana
Fresh weight (before)4.9 (0.6)3.6 (0.5)n/a2.7 (0.6)2.2 (0.4)
Fresh weight (after)2.9 (1.8)2.4 (0.6)n/a2.3 (0.7)1.6 (0.3)
Pontoscolex corethrurus
Fresh weight (before)2.0 (0.3)n/a1.5 (0.3)1.4 (0.1)1.2 (0.1)
Fresh weight (after)1.8 (0.4)n/a1.5 (0.1)1.7 (0.2)1.4 (0.2)
Capital letters (E, O, and P) represent treatments with different earthworm assemblages. Single-species: E = Estherella spp.; O = Onychochaeta borincana; P = Pontoscolex corethrurus. Two-species: E + O = Estherella spp. and O. borincana assemblage; E + P = Estherella spp. and P. corethrurus assemblage; O + P = O. borincana and P. corethrurus assemblage. Three-species: E + O + P = Estherella spp., O. borincana, and P. corethrurus assemblage. Value is shown as mean (S.D.) (n = 4) at the beginning of the experiment (before) and after the 22-day experiment (after). “n/a” indicates the particular earthworm species was not introduced into the corresponding experimental mesocosm.
Table 2. Total soil carbon (mg C/ g soil) and nitrogen (μg N/ g soil), atom percentages of 13C and 15N (%) and delta 13C (δ13C; ‰) and delta 15N (δ15N; ‰) from the initial soil samples (no isotope-labeled materials and no worms at Day 0; Initial), control treatment (no isotope-labeled materials and no worms at Day 22; Soil) and earthworm treatments at the end of the 22-day mesocosm experiment with Puerto Rican soils.
Table 2. Total soil carbon (mg C/ g soil) and nitrogen (μg N/ g soil), atom percentages of 13C and 15N (%) and delta 13C (δ13C; ‰) and delta 15N (δ15N; ‰) from the initial soil samples (no isotope-labeled materials and no worms at Day 0; Initial), control treatment (no isotope-labeled materials and no worms at Day 22; Soil) and earthworm treatments at the end of the 22-day mesocosm experiment with Puerto Rican soils.
Earthworm treatment
VariablesInitialSoilEOPE + OE + PO + PE + O + PStatistics
Soil Carbon
Total C39.6 (0.5)43.5 (2.5) 42.5 (3.7)43.8 (2.0)41.0 (1.6)42.9 (3.8)42.1 (2.7)42.0 (1.5)42.1 (2.2)F8, 27 = 1.0; p = 0.43
Atom 13C (%)1.0753 a (0.0001)1.0752 a (0.0002)1.0767 bc (0.0003)1.0771 abc (0.0009)1.0767 ac (0.0004)1.0768 abc (0.0002)1.0776 bc (0.0005)1.0786 b (0.0020)1.0769 abc (0.0007)F8, 27 = 7.2; p < 0.0001
δ13C−27.8 a (0.1)−27.9 a (0.2)−25.8 bc (0.3)−26.1 abc (0.9)−26.5 ab (0.4)−26.4 abc (0.2)−25.6 bc (0.4)−24.8 c (1.8)−26.3 abc (0.6)F8, 27 = 7.2; p < 0.0001
Soil Nitrogen
Total N371.5 (2.3)367.9 (19.0)375.0 (19.5)370.8 (21.4)364.3 (11.0)369.1 (19.6)362.3 (19.7)367.4 (11.4)365.6 (8.3)F8, 27 = 0.2; p = 0.9
Atom 15N (%)0.36815 a (0.00005)0.36810 a (0.00005)0.36885 ab (0.00042)0.36858 ab (0.00012)0.36866 ab (0.00036)0.36889 ab (0.00025)0.36885 ab (0.00004)0.36915 b (0.00072)0.36882 ab (0.00033)F8, 27 = 4.3; p = 0.002
δ15N4.6 a (0.1)4.5 a (0.2)6.5 ab (1.1)5.8 ab (0.3)6.0 ab (1.0)6.6 ab (0.7)6.5 ab (0.1)7.3 b (2.0)6.4 ab (0.9)F8, 27 = 4.3; p = 0.002
Capital letters (E, O, and P) represent treatments with different earthworm assemblages. Single-species: E = Estherella spp.; O = Onychochaeta borincana; P = Pontoscolex corethrurus. Two-species: E + O = Estherella spp. and O. borincana assemblage; E + P = Estherella spp. and P. corethrurus assemblage; O + P = O. borincana and P. corethrurus assemblage. Three-species: E + O + P = Estherella spp., O. borincana and P. corethrurus assemblage. Value is shown as mean (S.D.) (n = 4). Statistics shows the statistical results (F ratios and p values) from one-way ANOVA (GLM for unbalanced data). Different letters indicate significant difference among earthworm treatments (Tukey’s HSD, p < 0.05).
Table 3. Earthworm tissue total carbon (C) and nitrogen (N) percentages (%), atom percentages of 13C and 15N (%), and delta 13C (δ13C; ‰) and delta 15N (δ15N; ‰) in native earthworms Estherella spp. (E) and Onychochaeta borincana (O) at each earthworm mesocosm from different earthworm treatments at the end of the 22-day experiment with Puerto Rican soils.
Table 3. Earthworm tissue total carbon (C) and nitrogen (N) percentages (%), atom percentages of 13C and 15N (%), and delta 13C (δ13C; ‰) and delta 15N (δ15N; ‰) in native earthworms Estherella spp. (E) and Onychochaeta borincana (O) at each earthworm mesocosm from different earthworm treatments at the end of the 22-day experiment with Puerto Rican soils.
Earthworm treatments
VariablesSingle species (E or O)E + OE + PO + PE + O + PStatistics
Estherella spp.
Total C (%)46.3 (0.8)45.7 (1.3)46.2 (1.1)n/a47.2 (1.8)F3, 39 = 2.2; p = 0.10
Atom13C (%)1.0805 a (0.0039)1.0785 ab (0.0004)1.0781 b (0.0006)n/a1.0788 ab (0.0007)F3, 39 = 2.9; p = 0.047
δ13C−23.0 a (3.5)−24.8 ab (0.4)−25.2 b (0.5)n/a−24.6 b (0.7)F3, 39 = 2.9; p = 0.040
Total N (%)12.4 (0.5)12.3 (0.8)12.2 (1.0)n/a12.7 (0.4)F3, 39 = 0.8; p = 0.5
Atom15N (%)0.3690 (0.0002)0.3688 (0.0003)0.3689 (0.0004)n/a0.3688 (0.0002)F3, 39 = 1.0; p = 0.4
δ15N6.8 (0.6)6.2 (0.9)6.6 (1.0)n/a6.5 (0.6)F3, 39 = 1.0; p = 0.4
Onychochaeta borincana
Total C (%)46.0 (1.2)46.6 (1.5)n/a46.6 (1.3)46.5 (1.2)F3, 25 = 0.4; p = 0.8
Atom13C (%)1.0823 (0.0046)1.0812 (0.0016)n/a1.0845 (0.0102)1.0812 (0.0006)F3, 25 = 0.5; p = 0.7
δ13C−21.4 (4.2)−22.4 (1.5)n/a−19.3 (9.4)−22.3 (0.5)F3, 25 = 0.5; p = 0.7
Total N (%)11.8 (0.8)12.5 (0.7)n/a12.3 (0.7)12.4 (0.5)F3, 25 = 1.8; p = 0.2
Atom15N (%)0.3693 (0.0013)0.3694 (0.0006)n/a0.3705 (0.0035)0.3697 (0.0004)F3, 25 = 0.4; p = 0.7
δ15N8.69 (3.6)8.2 (1.6)n/a11.0 (9.5)8.9 (1.0)F3, 25 = 0.4; p = 0.7
Capital letters (E, O, and P) represent treatments with different earthworm assemblages. Single-species: E = Estherella spp.; O = Onychochaeta borincana; P = Pontoscolex corethrurus. Two-species: E + O = Estherella spp. and O. borincana assemblage; E + P = Estherella spp. and P. corethrurus assemblage; O + P = O. borincana and P. corethrurus assemblage. Three-species: E + O + P = Estherella spp., O. borincana and P. corethrurus assemblage. Value is shown as mean (S.D.). Statistics shows the statistical results (F ratios and p values) from one-way ANOVA (GLM for unbalanced data). Different letters indicate significant difference among earthworm treatments (Tukey’s HSD, p < 0.05).
Table 4. Earthworm tissue total carbon (C) and nitrogen (N) percentages (%), atom percentages of 13C and 15N (%) and delta 13C (δ13C; ‰) and delta 15N (δ15N; ‰) in native earthworms Estherella spp. (E) and Onychochaeta borincana (O) at each earthworm mesocosm from different earthworm treatments at the end of the 22-day experiment with Puerto Rican soils.
Table 4. Earthworm tissue total carbon (C) and nitrogen (N) percentages (%), atom percentages of 13C and 15N (%) and delta 13C (δ13C; ‰) and delta 15N (δ15N; ‰) in native earthworms Estherella spp. (E) and Onychochaeta borincana (O) at each earthworm mesocosm from different earthworm treatments at the end of the 22-day experiment with Puerto Rican soils.
Earthworm treatments
VariablesSingle species (P)PJE + PO + PE + O + PStatistics
Pontoscolex corethrurus
Total C (%)47.0 (1.0) a41.0 (4.7) b44.7 (6.1) ab46.3 (1.6) a46.9 (0.3) aF4, 52 = 3.9; p = 0.007
Atom13C (%)1.0809 a (0.0008)1.0791 b (0.0011)1.0812 a (0.0009)1.0813 a (0.0012)1.0812 a (0.0005)F 4, 52 = 4.8; p = 0.002
δ13C−22.6 a (0.8) −24.3 b (1.4)−22.4 a (0.8)−22.2 a (1.1)−22.3 a (0.5)F 4, 52 = 4.7; p = 0.002
Total N (%)11.9 (0.5) a9.2 (2.0) b11.3 (1.5) a11.4 (1.1) a11.9 (0.4) aF 4, 52 = 6.0; p < 0.001
Atom15N (%)0.3686 a (0.0001)0.3692 b (0.0003)0.3686 a (0.0002)0.3687 a (0.0003)0.3686 a (0.0001)F 4, 52 = 7.2; p < 0.001
δ15N5.9 (0.4) a7.6 (0.9) b5.9 (0.5) a6.1 (0.9) a5.9 (0.3) aF 4, 52 = 7.2; p < 0.001
Capital letters (E, O, and P) represent treatments with different earthworm assemblages. Single-species: E = Estherella spp.; O = Onychochaeta borincana; P = Pontoscolex corethrurus. Two-species: E + O = Estherella spp. and O. borincana assemblage; E + P = Estherella spp. and P. corethrurus assemblage; O + P = O. borincana and P. corethrurus assemblage. Three-species: E + O + P = Estherella spp., O. borincana and P. corethrurus assemblage. Value is shown as mean (S.D.). Statistics shows the statistical results (F ratios and p values) from one-way ANOVA (GLM for unbalanced data). Different letters indicate significant difference among earthworm treatments (Tukey’s HSD, p < 0.05).
Table 5. Microbial biomass total carbon (MBC, μg C /g soil), carbon-13C (MBC-13C; μg 13C /g soil), atom percentage of 13C (%), and soil delta 13C (δ13C; ‰), soil respiration C-CO2 (μg C per day), atom percentage of 13C-CO2 (%), and delta 13C-CO213C; ‰) from the control treatments (Soil Only, soil with 15N-labeled grass (Grass), soil with 13C-labeled leaf litter (Litter), and Control (soil with both grass and leaf litter but no worms)) and earthworm treatments at the end of the 22-day mesocosm experiment with Puerto Rican soils.
Table 5. Microbial biomass total carbon (MBC, μg C /g soil), carbon-13C (MBC-13C; μg 13C /g soil), atom percentage of 13C (%), and soil delta 13C (δ13C; ‰), soil respiration C-CO2 (μg C per day), atom percentage of 13C-CO2 (%), and delta 13C-CO213C; ‰) from the control treatments (Soil Only, soil with 15N-labeled grass (Grass), soil with 13C-labeled leaf litter (Litter), and Control (soil with both grass and leaf litter but no worms)) and earthworm treatments at the end of the 22-day mesocosm experiment with Puerto Rican soils.
Earthworm Treatments
VariablesSoil OnlyGrassLitterControlEOPE + OE + PO + PE + O + PStatistics
Microbial biomass
MBC741.3 (103.0)570.2 (167.9)568.3 (166.3)332.1 (183.2)659.8 (119.2)340.1 (115.3)528.8 (91.4)479.4 (119.2)448.1 (110.3)483.4 (199.5)431.7 (224.4)F10,29 = 1.3; p = 0.26
MBC-13C8.0 (1.1)6.2 (1.3)6.2 (1.1)3.6 (1.3)7.2 (1.3)3.7 (1.2)5.7 (1.0)5.2 (1.3)4.9 (1.1)5.3 (2.2)4.7 (1.1)F10, 29 = 1.3; p = 0.27
Atom13C (%)1.078 a (0.002)1.079 a (0.0004)1.083 ab (0.004)1.09 b (0.009)1.083 ab (0.003)1.082 ab (0.003)1.086 ab (0.004)1.085 ab (0.002)1.083 ab (0.002)1.086 ab (0.004)1.086 ab (0.003)F10, 29 = 2.8; p = 0.015
δ13C−36.1 a (1.4)−34.9 ab (0.4)−31.1 ab (3.5)−30.6 ab (1.4)−31.1 ab (2.3)−32.0 ab (2.9)−28.8 b (3.4)−29.4 ab (1.8)−31.5 ab (1.6)−28.8 b (3.4)−29.1 b (2.5)F10, 29 = 3.3; p = 0.006
VariablesSoil OnlyGrassLitter ControlEOPE + OE + PO + PE + O + PStatistics
Soil respiration at day 21
C-CO21.73 a (0.79)3.87 ab (0.91)5.24 abc (0.92)9.51 c (4.95)8.01 bc (2.05)6.35 abc (1.58) 9.32 bc (1.50)9.50 c (0.99)8.90 bc (1.09)9.99 c (3.17)7.88 bc (2.23)F10, 32 = 5.2; p < 0.001
13C- CO2 (%)1.085 a (0.002)1.088 a (0.004)1.228 b (0.014)1.223 b (0.012)1.206 bc (0.020)1.209 bc (0.004)1.220 b (0.023)1.205 bc (0.007)1.215 bc (0.018)1.183 c (0.008)1.195 bc (0.010)F10, 32 = 53.6; p < 0.0001
δ13C−18.8 a (2.1)−16.5 a (3.6)111.9 b (13.1)107.5 b (11.3)91.7 bc (18.7)94.3 bc (3.3)104.9 b (21.2)91.3 bc (6.9)100.2 bc (16.9)71.1 c (7.1)81.8 bc (8.9)F10, 32 = 53.5; p < 0.0001
Capital letters (E, O, and P) represent treatments with different earthworm assemblages. Single-species: E = Estherella spp.; O = Onychochaeta borincana; P = Pontoscolex corethrurus. Two-species: E + O = Estherella spp. and O. borincana assemblage; E + P = Estherella spp. and P. corethrurus assemblage; O + P = O. borincana and P. corethrurus assemblage. Three-species: E + O + P = Estherella spp., O. borincana and P. corethrurus assemblage. Value is shown as mean (S.D.) (n = 4, except data with: n = 3). Statistics shows the statistical results (F ratios and p values) from one-way ANOVA (GLM for unbalanced data). Different letters indicate significant difference among earthworm treatments (Tukey’s HSD, p < 0.05).
Table 6. Soil microbial total nitrogen (MBN; μg N/g soil), atom percentage of 15N (MBN-15N; %), and delta15N (δ15N; ‰) signature and dissolved inorganic nitrogen (DIN; μg N/g soil), and atom percentage of 15N (DIN-15N; %) in DIN from the control treatments (Soil Only, soil with 15N-labeled grass (Grass), soil with 13C-labeled leaf litter (Litter), and Control (soil with grass and leaf litter but no worms)) and earthworm treatments at the end of the 22-day mesocosm experiment with Puerto Rican soils. See Table 5 for definitions of abbreviations.
Table 6. Soil microbial total nitrogen (MBN; μg N/g soil), atom percentage of 15N (MBN-15N; %), and delta15N (δ15N; ‰) signature and dissolved inorganic nitrogen (DIN; μg N/g soil), and atom percentage of 15N (DIN-15N; %) in DIN from the control treatments (Soil Only, soil with 15N-labeled grass (Grass), soil with 13C-labeled leaf litter (Litter), and Control (soil with grass and leaf litter but no worms)) and earthworm treatments at the end of the 22-day mesocosm experiment with Puerto Rican soils. See Table 5 for definitions of abbreviations.
Earthworm Treatments
VariablesSoil OnlyGrassLitterControlEOPE + OE + PO + PE + O + PStatistics
Microbial biomass
MBN124.6 (30.1)96.8 (26.8)110.2 (25.5)129.1 (54.5)190.4 (110.2)114.5 (31.0)162.1 (65.0)92.3 (27.9)111.0 (39.0)90.4 (21.9)136.9 (74.3)F10,31 = 1.2; p = 0.3
MBN-15N (%)0.3691 a (0.0005)0.3747 b (0.0017)0.3693 a (0.0007)0.3708 a (0.0019)0.3709 a (0.0019)0.3694 a (0.0012)0.3711 a (0.0017)0.3721 ab (0.0015)0.3709 a (0.0004)0.3711 a (0.0008)0.3698 a (0.0001)F10, 31 = 6.0; p < 0.0001
δ15N7.5 a (1.3)23.0 b (4.8)8.1 a (1.9)12.3 a (5.3)12.7 a (5.3)8.5 a (3.4)12.0 a (4.7)15.7 ab (4.1)12.5 a (1.2)13.2 a (2.3)9.4 a (0.1)F10, 31 = 6.0; p < 0.0001
Dissolved inorganic N
DIN62.9 a (12.8)37.0 b (8.9)22.6 b (8.4)18.4 b (4.1)40.4 ab (8.6)38.8 ab (20.2)23.8 b (7.7)31.1 b (6.7)25.7 b (6.4)28.8 b (7.1)33.0 b (6.2)F10, 31 = 5.7; p < 0.0001
DIN-15N (%)0.3692 a (0.0008)0.3958 b (0.0149)0.3687 a (0.0003)0.3740 a (0.0003)0.3770 a (0.0041)0.3749 a (0.0025)0.3751 a (0.0087)0.3784 a (0.0046)0.3749 a (0.0025)0.3813 ab (0.0076)0.3776 a (0.0043)F10, 31 = 6.4; p < 0.0001
Value is shown as mean (S.D.) (n = 4, except data with: n = 3). Statistics shows the statistical results (F ratios and p values) from one-way ANOVA (GLM for unbalanced data; significant level α = 0.05).

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Huang, C.-Y.; González, G.; Hendrix, P.F. Resource Utilization by Native and Invasive Earthworms and Their Effects on Soil Carbon and Nitrogen Dynamics in Puerto Rican Soils. Forests 2016, 7, 277. https://doi.org/10.3390/f7110277

AMA Style

Huang C-Y, González G, Hendrix PF. Resource Utilization by Native and Invasive Earthworms and Their Effects on Soil Carbon and Nitrogen Dynamics in Puerto Rican Soils. Forests. 2016; 7(11):277. https://doi.org/10.3390/f7110277

Chicago/Turabian Style

Huang, Ching-Yu, Grizelle González, and Paul F. Hendrix. 2016. "Resource Utilization by Native and Invasive Earthworms and Their Effects on Soil Carbon and Nitrogen Dynamics in Puerto Rican Soils" Forests 7, no. 11: 277. https://doi.org/10.3390/f7110277

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