Coral kin aggregations exhibit mixed allogeneic reactions and enhanced fitness during early ontogeny
© Amar et al; licensee BioMed Central Ltd. 2008
Received: 08 January 2008
Accepted: 30 April 2008
Published: 30 April 2008
Aggregated settlement of kin larvae in sessile marine invertebrates may result in a complex array of compatible and incompatible allogeneic responses within each assemblage. Each such aggregate can, therefore, be considered as a distinct self-organizing biological entity representing adaptations that have evolved to maximize the potential benefits of gregarious settlement. However, only sparse information exists on the selective forces and ecological consequences of allogeneic coalescence.
We studied the consequences of aggregated settlement of kin larvae of Stylophora pistillata (a Red Sea stony coral), under controlled laboratory settings. When spat came into contact, they either fused, establishing a chimera, or rejected one another. A one-year study on growth and survivorship of 544 settled S. pistillata genotypes revealed six types of biological entities: (1) Single genotypes (SG); (2) Bi-chimeras (BC); (3) Bi-rejecting genotypes (BR); (4) Tri-chimera entities (TC); (5) Three-rejecting genotypes (TR); and (6) Multi-partner entities (MP; consisting of 7.5 ± 2.6 partners). Analysis of allorecognition responses revealed an array of effector mechanisms: real tissue fusions, transitory fusions and six other histoincompatible reactions (borderline formation, sutures, overgrowth, bleaching, rejection, and partner death), disclosing unalike onsets of ontogeny and complex modes of appearance within each aggregate. Evaluations at the entity level revealed that MP entities were the largest, especially in the first two months (compared with SG: 571% in the first month and 162% in the seventh month). However, at the genotype level, the SG entities were the largest and the colonies with the highest-cost-per-genotype were the TR and the MP colonies. The cost was calculated as reduced average genotype size, from 27% and 12% in the first month to 67% and 64% in the seventh month, respectively. In general, MP exhibited the highest survivorship rate (85%, after one year) and SG the lowest (54%).
In view of the above, we suggest that the driving force behind gregarious kin settlements in Stylophora pistillata stems from gained benefits associated with the immediate and long-term increase in total size of the MP entity, whereas survivorship rates did not draw a parallel link. Furthermore, the biological organization of MP entity exhibits, simultaneously, an intricate network of rejecting and fusible interactions in a single allogeneic intimate arena, where proposed benefits surpass costs incurred by discord among founders. Above results and documentations on gregarious settlement in other marine taxa bring us to suggest that the 'group level' of kin aggregates may serve as a ubiquitous legitimate selection entity in the evolution of a sessile mode of life in marine organisms.
Natural chimerism, the biological state in which an organismal entity comprises cell populations originating from more than a single distinct fertilization product , is documented in a wide range of organisms including protists, animals and plants [2–10]. However, it is commonly perceived that the reverse situation, cellular uni-clonality within a biological entity, is a key evolutionary tool for prevention of inner-organism conflict and cellular pervasiveness [11, 12]. Although research on animal and plant chimerism dates back to the early twentieth century [13, 14], it is surprising that only sparse information exists on the ecological costs and benefits of genetically non-homogeneous biological entities. On one hand, vertebrate and invertebrate chimeras have been found to carry significant costs. Studies on invertebrates showed reduced growth rates, morphological resorption and necrosis [6, 8, 15, 16]. In vertebrates, autoimmune diseases, freemartins and other abnormal syndromes have been recorded . The literature also documents the expression of somatic and germ cell parasitism in vertebrates and invertebrates alike [1, 4, 10, 17–19]. Various experimental manipulations during vertebrate and invertebrate development have revealed natural chimerism, often at early stages of ontogeny [1, 6, 15, 20]. This phenomenon is enhanced in some sessile marine invertebrates by the gregarious co-settlement of larvae [15, 21, 22]. The above outcomes raise a critical question: What selective forces favour natural chimerism, in which there are so many 'losers' and so much to lose?
Some studies on aggregated settlement and chimerism have attributed an assortment of advantages in hard and soft corals [5, 15, 22], sponges [23, 24], bryozoans , hydrozoans , and ascidians . These include the expression of heterosis, increased genetic repertoire, reduced onset of reproduction, increased competitive capabilities, enhanced growth and survivorship rates, synergistic complementation and assurance of mate location [4, 27–34]. Similar conclusions followed the formation of differentiated multicellular slugs by aggregates of social amoebae .
Gregarious co-settlement of conspecific larvae [13, 15, 22, 28] creates suitable conditions for the development of a complex array of both compatible and incompatible allogeneic responses, because the genotypes within each chimeric entity or the rejecting partners within an aggregate are engaged in several types of allogeneic encounters. It is therefore possible to consider an entire aggregate of co-settled larvae (and its multiple allogeneic responses) as a self-organizing distinct biological entity, and inquire if adaptations have evolved to maximize the potential benefits of their gregarious settlement.
Observations (B. Rinkevich, unpubl.) documented in the wild, frequent aggregated spat of the Red Sea branching coral Stylophora pistillata. In order to elucidate the costs and benefits (in terms of growth and survival) of various types of such assemblages, we examined in controlled laboratory settings, the outcomes of six different classes of aggregates of settled kin larvae and their alloimmune responses in young S. pistillata colonies for up to one year. Interactions among spat of S. pistillata revealed various levels of costs and benefits for mixed alloimmune contacts within each aggregate. We therefore conclude that the 'group level' of kin aggregates may act as a legitimate selection entity in sessile marine organisms that settle gregariously.
Summary of the onset of allogeneic outcomes between young kin colonies of Stylophora pistillata.
Order of allogeneic mechanism
Number of allogeneic interactions that exhibited each mechanism of rejection (% of total interactions in each order) (% of total rejections in each order)
Organismal uniclonality is assumed to be beneficial in preventing inner-organism conflicts [11, 12]. Therefore, the occurrence in nature of genetically non-homogeneous entities (chimeras) in a variety of protists, fungi, plants and animals is perplexing ([2–6, 8, 10, 15] and literature therein). The occurrence of chimeras also challenges the paradigm for evolutionary benefits associated with genetically homogeneous multicellular organisms [7, 9, 10, 37], the traditional notion of the unit of selection [7, 37], and our perception of multicellular stability [33, 34, 38]. The scientific literature attributes many benefits to the state of chimerism [4, 16, 27–34], especially in cases of fusion between kin, rationalizing a chimera as a congruent entity . However, if coral planulae are gregarious settlers, then they may fuse by virtue of physical proximity regardless of selective advantage. It is therefore natural to ask, is chimerism in the stony coral Stylophora pistillata evolutionarily beneficial? How shall we consider cases where, in addition to chimerism, a gregarious settlement may create groups of kin organisms, each exhibiting concurrently an intricate network of rejecting and fusible interactions?
Given the meagre knowledge on coral population genetics and the limited competency for genetic discrimination, the currently available molecular tools do not allow the evaluation of genetic relatedness in natural coalescences. We chose to analyse kin aggregates in a laboratory, where replicates can be generated with tens of planulae per Petri dish. Under our controlled laboratory conditions, Stylophora pistillata sibling larvae had a single ontogenic opportunity to choose whether to live in an aggregate. Most larvae (67%) selected the option of co-settlement and kin intimacy . Each established kin aggregate of coral spat exhibited mixed allogeneic responses, from true tissue fusion to rejection, and ending in tissue necrosis and colony death. Such an aggregates mode of settlement, which leads to a variety of simultaneously-developing allogeneic encounters, is unlikely to occur unless selective pressure favours its existence . Our study reveals that the common formation of multi-partner (MP) entities implicates the 'group level' (an assemblage of several genotypes, both rejecting and fusing, in one entity) as a key level at which natural selection may occur. Our results at the group level contradicted our genotype-level results. The mixed-allogeneic MP entity in this study (7.5 ± 2.6 partners) was, in its first month, 6.7 times larger than the single genotype (SG) entity. This consistently decreased to a ratio of only 2.6 at the age of seven months. On the genotype level, the areal sizes of SG colonies were 1.1 times larger than MP genotypes in the first month, and this trend increased consistently to 2.8 times at the age of seven months. We propose, therefore, that the benefit of being a partner in a MP entity (either engaged with rejection or fusion interactions) lays in the sensitive early phases of ontogeny, in which the ability to reach rapidly a large size and to occupy a large substrate space relative to other individuals is subject to intense selection pressure in sessile marine invertebrates (sensu; [4, 27, 28]). Successful long-term control of a feeding substrate by large MP entities of Stylophora pistillata effectively prevents colonization of this surface area by other competing taxa, and likely increases competitiveness toward existing neighbours. Since kin larvae form aggregates preferentially , the establishment of MP entities, while it minimizes space exploitation by each settling genotype, may increase the inclusive fitness of close relatives within each aggregate.
The maintenance of MP entities comes at a cost. Calculations made at the genotype level revealed a single genotype size cost ranging from 12% (in the first month) to 64% (in the seventh month). This was not the case with the smaller aggregates tested; the costs of maintenance of bi-chimeras (BC) and tri-chimeras (TC) at the genotype level were low compared to SG colonies, ranging from a benefit of 12% in the first month to a cost of 22% in the seventh month in BC colonies, and costs of 8%–46% in TC. These results contrast with known outcomes for BC and TC entities in colonial urochordates (Botryllus schlosseri, [16, 39, 40]).
There are numerous documented costs of genetically non-homogenous entities in sedentary marine organisms. These include reduced chimeric sizes in sponges  and soft corals , polyp/zooid resorptions in soft corals  and colonial tunicates [32, 42], unstable entities in scleractinian corals , somatic and germ cell parasitism in botryllid ascidians [1, 10, 17, 18] and decreased survivorship in tunicates [16, 32, 33]. However, when dealing with MP entities, laboratory studies on the tunicates Botryllus schlosseri  and Botrylloides leachi  revealed that multi-chimeras were more stable, grew faster, and had lower frequencies of colony resorption compared to bi-chimeras. In corals, multi-partner chimeras of Pocillopora damicornis were the largest entities among individual, bichimera and non-fused colonies, and with the highest survival rates , recalling our results here for survival. The evolutionary advantages of aggregated vs. solitary biological situations can be puzzling, and should be examined not only in the allorecognition context as depicted here, but also in other biological scenarios, such as the hatching success of solitary vs. aggregated nest events in marine turtles .
In conclusion, we reveal here that a driving force for gregarious kin entities, which develop by sedentary marine organisms like cnidarians [5, 13, 22] and urochordates , may stem from the benefits in terms of the total size of the aggregated entity, which includes rejecting and fusing partners. Therefore, in addition to previous studies suggesting that selection operates at the colony level , it is important also to consider the 'group level' of kin aggregates (revealing a network of historecognition responses) as a legitimate selection entity in the biology and ecology of sessile marine organisms. In such entities, intraspecific cooperation among kin may develop [10, 27, 39]. Explicit work should further consider arenas of non-related genotypes under laboratory conditions and when possible, in situ coalescences, where different genotypes simultaneously cooperate and compete under natural conditions.
Planula larvae were collected in situ (March and April 2005; [6, 22, 45]) from 10 gravid colonies of Stylophora pistillata on the coral reef adjacent to the Interuniversity Institute for Marine Sciences (IUI, Eilat, Red Sea), and shipped to the laboratory at Israel Oceanographic and Limnological Research (IOLR, Haifa) within two days after collection. Planula settlement began within several hours post-collection and continued for up to three weeks. Groups of 50–70 planulae, each hatched from a single mother colony, were placed in polyester film lined, 60 mm Petri dishes, each containing 45 ml seawater (under these conditions the percentages of planulae that aggregate do not correlate with density; ). Under these conditions, 67% of the kin planulae settled in aggregations (spat <1 mm from each other) of at least two spat per aggregate, while the rest (33%) settled solitarily. Upon settlement, each individual spat or aggregated entity was numbered by pencil on the polyester film. Next, the surrounding film was trimmed, leaving each young colony on a small disc of film, which then was attached by cyanoacrylate glue (Super Glue 3, Loctite, Ireland) to a 5.0 × 7.5 cm glass slide. Detailed rearing methods for these young corals under laboratory conditions are described elsewhere [22, 45]. In total, we monitored 544 metamorphosed larvae produced by 10 S. pistillata colonies.
First, we randomly selected 208 spat to measure growth, because it was logistically impossible to record the growth of all coral spat due to sampling time constraints. These spat were examined carefully each month for the next seven months. Spat were assigned to six entity classes according to the number of partners within each aggregation and their allorecognition response types: (1) Single genotypes (SG, n = 12, Fig. 1a); (2) Bi-chimeras, each consisting of two fused genotypes (BC, n = 11, Fig. 1b); (3) Bi-rejecting genotypes (BR, n = 11, Fig. 1c), (4) Tri-chimeras, each of three fused genotypes (TC, n = 7, Fig. 1d); (5) Tri-rejecting genotypes (TR, n = 16, Fig. 1e); and (6) Multi-partner entities that included both fusion and rejection patterns (MP, n = 11, Fig. 1f), each containing, at least, three fused partners (maximum number of 12 partners per aggregate, mean ± SD, 7.5 ± 2.6 partners, Fig. 1f). Costs and benefits were calculated for each of these six response types, in terms of growth in surface area, as a percent difference from the average surface area of SG entities, on the level of both whole entities and genotypes.
Next, we documented the survival rate of all 544 spat that settled both as individuals and in aggregates, each month for the first seven months and then again at the age of 12 months. Survival was determined for 113 SG, 48 BC, 51 BR, 16 TR, 34 TC, and 26 MP entities (n = 288 total entities and n = 544 total spat, since most entities contained >one coral spat). Each entity in the six classes containing more than a single genotype, was developed, from groups of planulae originated from a single mother colony. Data for spats from 10 maternal colonies in each class was pooled as no significant difference was recorded in the growth rates between the colonies within each class (One-way ANOVA, F = 1.3, p > 0.05) and survivorship of young spats was not affected by the mother origin (p > 0.05).
Then, we monitored the development of allorecognition in 223 randomly-selected S. pistillata spat for up to one year. These spat included some that were monitored for growth above, and some that were not. Four classes of entities were observed to determine the development of effector mechanisms: 33 BC, 35 BR, 9 TC and 20 TR. Multi-partner entities were not included in this experiment, because of the difficulty of monitoring simultaneously several different allogeneic interactions in each genotype. A state of true allogeneic fusion was recorded when fused partners remained continuously connected by intact tissue during the entire experimental period. A state of transitory fusion was recorded when partners initially appeared to undergo tissue fusion, but later developed an incompatible reaction. Six other morphological outcomes developed directly as incompatible effector mechanisms: (1) a borderline between contacting genotypes, without any sign of tissue necrosis; (2) suture formation  between partners, marked by a thin skeletal wall; (3) overgrowth, in which one genotype overgrew its confrere; (4) bleaching, in which a white region demarcated the interacting partners; (5) tissue necrosis followed by separation between the partners; and (6) death of one of the partners. We monitored the development of these allorecognition interactions over time. The order in which one transitioned to another was numbered, as well as the age at which each transition occurred.
Colonies were observed each week under a Nikon SMZ800 stereomicroscope. Photographs (once every two weeks during the first two months, and thereafter once per month) were taken with a Color View 2 Soft Imagin System camera equipped with a millimeter grid as a scale bar.
Data were analyzed statistically using SPSS software version 10 for Windows. Normality and homogeneity of variance were tested by Kolmogorov-Smirnov and Levene's statistical tests, respectively. ANOVAs followed by Duncan's post hoc tests were used for comparing the growth of the entity types, the ages at which the six allogeneic interactions occurred, and the order of development of allogeneic interactions. Chi square tests were used for evaluating survival rate. The results are presented as mean ± SD except where indicated.
We thank E. Reem, A. Lotan and I. Izhaki for assistance with statistical analysis, E. Kramarsky-Winter for helpful discussions in initial stages of the study, A. Alamaro for help with planulae collection and the IUI staff for use of facilities. This study was supported by the INCO-DEV project (REEFRES, no. 510657), CORALZOO, an EC Collective Research project (no. 012547), the AID-CDR program (no. C23-004), and Auburn University. This research fulfils part of the requirements for the doctoral degree by K. O. Amar at Bar Ilan University.
- Rinkevich B: Human natural chimerism: An acquired character or a vestige of evolution?. Human Immunol. 2001, 62: 651-657. 10.1016/S0198-8859(01)00249-X.View ArticleGoogle Scholar
- Gill TJ: Chimerism in humans. Transplant Proc. 1977, 9: 1423-17431.PubMedGoogle Scholar
- Benirschke K: Hermaphoridites, freemartins, mosaics and chimeras in animals. Mechanisms of Sex Differentiation in Animals and Man. Edited by: Austin CR, Edwards RG. 1981, New York, Academic Press, 421-463.Google Scholar
- Buss LW: Somatic cell parasitism and the evolution of somatic tissue compatibility. Proc Natl Acad Sci USA. 1982, 79: 5337-5341. 10.1073/pnas.79.17.5337.PubMed CentralView ArticlePubMedGoogle Scholar
- Hidaka M: Tissue compatibility between colonies and between newly settled larvae of Pocillopora damicornis. Coral Reefs. 1985, 4: 111-114. 10.1007/BF00300869.View ArticleGoogle Scholar
- Frank U, Oren U, Loya Y, Rinkevich B: Alloimmune maturation in the coral Stilophora pistillata is achieved through three distinctive stages, 4 month post-metamorphosis. Proc R Soc Lond B. 1997, 264: 99-104. 10.1098/rspb.1997.0015.View ArticleGoogle Scholar
- Rinkevich B: A critical approach to the definition of Darwinian units of selection. Biol Bull. 2000, 199: 231-240. 10.2307/1543179.View ArticlePubMedGoogle Scholar
- Rinkevich B: The colonial urochordate Botryllus schlosseri: from stem cells and natural tissue transplantation to issues in evolutionary ecology. BioEssays. 2002, 24: 730-740. 10.1002/bies.10123.View ArticlePubMedGoogle Scholar
- Rinkevich B: Will two walk together, except they have agreed?. J Evol Biol. 2004, 17: 1178-1179. 10.1111/j.1420-9101.2004.00809.x.View ArticlePubMedGoogle Scholar
- Rinkevich B: Natural chimerism in colonial urochordates. J Exp Mar Biol Ecol. 2005, 322: 93-109. 10.1016/j.jembe.2005.02.020.View ArticleGoogle Scholar
- Dawkins R: Parasites, desiderata lists and the paradox of the organism. Parasitology. 1990, 100: S63-S73.View ArticlePubMedGoogle Scholar
- Pal C, Papp B: Selfish cells threaten multicellular life. Trends Ecol Evol. 2000, 15: 351-352. 10.1016/S0169-5347(00)01932-7.View ArticlePubMedGoogle Scholar
- Duerden JE: Aggregated colonies in Madreporarian corals. Am Nat. 1902, 36: 461-471. 10.1086/278152.View ArticleGoogle Scholar
- Bankroft FW: Variation and fusion in compound ascidians. Proc California Acad Sci. 1903, 3: 137-186.Google Scholar
- Barki Y, Gateno D, Graur D, Rinkevich B: Soft coral natural chimerism: A window in ontogeny allows the creation of entities, compounding incongruous parts. Mar Ecol Prog Ser. 2002, 231: 91-99. 10.3354/meps231091.View ArticleGoogle Scholar
- Chadwick-Furman NE, Weissman IL: Effects of allogeneic contact on life history traits of the colonial ascidian Botryllus schlosseri in Monterey Bay. Biol Bull. 2003, 205: 133-143. 10.2307/1543234.View ArticlePubMedGoogle Scholar
- Pancer Z, Gershon H, Rinkevich B: Coexistence and possible parasitism of somatic and germ cell lines in chimeras of the colonial urochordate Botryllus schlosseri. Biol Bull. 1995, 189: 106-112. 10.2307/1542460.View ArticleGoogle Scholar
- Stoner DS, Rinkevich B, Weissman IL: Heritable germ and somatic cell lineage competitions in chimeric colonial protochordates. Proc Natl Acad Sci USA. 1999, 96: 9148-9153. 10.1073/pnas.96.16.9148.PubMed CentralView ArticlePubMedGoogle Scholar
- Souter VL, Parisi MA, Nyholt DR, Kapur RP, Henders AK, Opheim KE, Gunther DF, Mitchell ME, Glass IA, Montgomery GW: A case of true hermaphroditism reveals an unusual mechanism of twinning. Human Genet. 2007, 179-185. 10.1007/s00439-006-0279-x.Google Scholar
- Nozawa Y, Loya Y: Genetic relationship and maturity state of the allorecognition system affect contact reactions in juvenile Seriatopora corals. Mar Ecol Prog Ser. 2005, 286: 115-123. 10.3354/meps286115.View ArticleGoogle Scholar
- Grosberg RK, Quinn JF: The genetic control and consequences of kin recognition by the larvae of a colonial marine invertebrate. Nature. 1986, 322: 456-459. 10.1038/322456a0.View ArticleGoogle Scholar
- Amar KO, Chadwick NE, Rinkevich B: Coral planulae as dispersion vehicles: biological properties of larvae released early and late in the season. Mar Ecol Prog Ser. 2007, 350: 71-78. 10.3354/meps07125.View ArticleGoogle Scholar
- Ilan M, Loya Y: Ontogenic variation in sponge histocompatibility responses. Bid Bull. 1990, 179: 279-286. 10.2307/1542319.View ArticleGoogle Scholar
- McGhee KE: The importance of life history stage and individual variation in the allorecognition system of a marine sponge. J Exp Mar Biol Ecol. 2006, 333: 241-250. 10.1016/j.jembe.2005.12.050.View ArticleGoogle Scholar
- Hughes RN, Manriquez PH, Morley S, Craig SF, Bishop JD: Kin or self-recognition? Colonial fusibility of the bryozoan Celleporella hyalina. Evol Dev. 2004, 6: 431-437. 10.1111/j.1525-142X.2004.04051.x.View ArticlePubMedGoogle Scholar
- Gild S, Frank U, Mokady O: Allogeneic interactions in Hydractinia: is the transitory chimera beneficial?. Int J Dev Biol. 2003, 47: 433-438.PubMedGoogle Scholar
- Buss LW: Group leaving, competition, and evolution of cooperation in a sessile invertebrate. Science. 1981, 213: 1012-1014. 10.1126/science.213.4511.1012.View ArticlePubMedGoogle Scholar
- Grosberg RK: The evolution of allorecognition specifity in clonal invertebrates. Q Rev Bio. 1988, 63: 377-412. 10.1086/416026.View ArticleGoogle Scholar
- Rinkevich B, Saito Y, Weissman IL: A colonial invertebrate species that displays a hierarchy of allorecognition responses. Biol Bull. 1993, 184: 79-86. 10.2307/1542381.View ArticleGoogle Scholar
- Rinkevich B: Bi-vs multi-chimerism in colonial urochordates: a hypothesis for links between natural tissue transplantation allogenetics and evolutionary ecology. Exp Clin Immunogenet. 1996, 13: 61-69.PubMedGoogle Scholar
- Foster KR, Fortunato A, Strassmann JE, Queller DC: The costs and benefits of being a chimera. Proc Biol Sci. 2002, 269: 2357-2362. 10.1098/rspb.2002.2163.PubMed CentralView ArticlePubMedGoogle Scholar
- Rinkevich B, Weissman IL: Chimeras in colonial invertebrates: a synergistic symbiosis or somatic and germ parasitism?. Symbiosis. 1987, 4: 117-134.Google Scholar
- Rinkevich B, Weissman IL: Chimeras vs genetically homogeneous individuals: potential fitness costs and benefits. Oikos. 1992, 63: 119-124. 10.2307/3545520.View ArticleGoogle Scholar
- Rinkevich B, Yankelevich I: Environmental split between germ cell parasitism and somatic cell synergism in chimeras of a colonial urochordate. J Exp Biol. 2004, 207: 3531-3536. 10.1242/jeb.01184.View ArticlePubMedGoogle Scholar
- Grigg RW: Resource menegment of precious corals: a review and application to shallw water reef building corals. Mar Ecol. 1984, 5: 57-74. 10.1111/j.1439-0485.1984.tb00307.x.View ArticleGoogle Scholar
- Hidaka M, Yurugi K, Sunagawa S, Kinzie RA: Contact reactions between young colonies of the coral Pocillopora damicornis. Coral Reefs. 1997, 16: 13-20. 10.1007/s003380050054.View ArticleGoogle Scholar
- Rinkevich B: Germ cell parasitism as an ecological and evolutionary puzzle: Hitchhiking with positively selected genotypes. Oikos. 2002, 96: 25-30. 10.1034/j.1600-0706.2002.960102.x.View ArticleGoogle Scholar
- Simon-Blecher N, Achituv Y, Rinkevich B: Protocordate concordant xenotransplantation settings reveal outbreaks of donor cells and divergent life span traits. Dev Comp Immunol. 2004, 28: 983-991. 10.1016/j.dci.2004.04.003.View ArticlePubMedGoogle Scholar
- Rinkevich B, Shapira M: Multi-partner urochordate chimeras outperform two-partner chimerical entities. Oikos. 1999, 87: 315-310. 10.2307/3546746.View ArticleGoogle Scholar
- Paz G, Rinkevich B: Morphological consequences for multi-partner chimerism in Botrylloides, a colonial urochordate. Dev Comp Immunol. 2002, 26: 615-622. 10.1016/S0145-305X(02)00022-8.View ArticlePubMedGoogle Scholar
- Vyver Van De S, Holvoet PD: Immunology and Parasitology. Variability of the immune response in freshwater sponges. J Exp Zool. 1990, 125: 215-227. 10.1002/jez.1402540214.View ArticleGoogle Scholar
- Rinkevich B, Weissman IL, Shapira M: Alloimmune hierarchies and stress-induced reversals in the resorption of chimeric protochordate colonies. Proc Roy Soc Lond B. 1994, 258: 215-220. 10.1098/rspb.1994.0165.View ArticleGoogle Scholar
- Raymundo A, Maypab AP: Getting bigger faster: mediation of size-specific mortality via fusion in juvenile coral transplants. Ecol Appl. 2004, 14: 281-295. 10.1890/02-5373.View ArticleGoogle Scholar
- Clusella-Trullas S, Paladino FV: Micro-environment of olive ridley turtle nests deposited during an aggregated nesting event. J Zool. 2007, 272: 367-376. 10.1111/j.1469-7998.2006.00277.x.View ArticleGoogle Scholar
- Amar KO, Rinkevich B: A floating mid-water coral nursery as larval dispersion hub: testing an idea. Mar Biol. 2007, 151: 713-718. 10.1007/s00227-006-0512-0.View ArticleGoogle Scholar
- Chadwick-Furman N, Rinkevich B: A complex allorecognition system in a reef-building coral: Delayed responses, reversals and nontransitive hierarchies. Coral Reefs. 1994, 13: 57-63. 10.1007/BF00426436.View ArticleGoogle Scholar